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. 2013 Nov 19;3(11):e325.
doi: 10.1038/tp.2013.100.

Genetic risk factors in two Utah pedigrees at high risk for suicide

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Genetic risk factors in two Utah pedigrees at high risk for suicide

H Coon et al. Transl Psychiatry. .

Abstract

We have used unique population-based data resources to identify 22 high-risk extended pedigrees that show clustering of suicide over twice that expected from demographically adjusted incidence rates. In this initial study of genetic risk factors, we focused on two high-risk pedigrees. In the first of these (pedigree 12), 10/19 (53%) of the related suicides were female, and the average age at death was 30.95. In the second (pedigree 5), 7/51 (14%) of the suicides were female and the average age at death was 36.90. Six decedents in pedigree 12 and nine in pedigree 5 were genotyped with the Illumina HumanExome BeadChip. Genotypes were analyzed using the Variant Annotation, Analysis, and Search program package that computes likelihoods of risk variants using the functional impact of the DNA variation, aggregative scoring of multiple variants across each gene and pedigree structure. We prioritized variants that were: (1) shared across pedigree members, (2) rare in other Utah suicides not related to these pedigrees, (3) < or = 5% in genotyping data from 398 other Utah population controls and (4) < or = 5% frequency in publicly available sequence data from 1358 controls and/or in dbSNP. Results included several membrane protein genes (ANO5, and TMEM141 for pedigree 12 and FAM38A and HRCT1 for pedigree 5). Other genes with known neuronal involvement and/or previous associations with psychiatric conditions were also identified, including NFKB1, CASP9, PLXNB1 and PDE11A in pedigree 12, and THOC1, and AUTS2 in pedigree 5. Although the study is limited to variants included on the HumanExome BeadChip, these findings warrant further exploration, and demonstrate the utility of this high-risk pedigree resource to identify potential genes or gene pathways for future development of targeted interventions.

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Figures

Figure 1
Figure 1
High-risk pedigree 12 and high-risk pedigree 5. Suicide cases that are shaded in red are those who have DNA samples collected by the OME; cases shaded in black are suicides known from death certificate data, but do not have DNA. In pedigree 12, for the three siblings on the left side, the suicides were separated by 6–26 years. The parent–child suicides on the right side of the pedigree are separated by 22 years. In pedigree 5, the half-sib suicides on the left side are separated by 6 years. The parent–child suicides in the center of pedigree 5 are separated by 13 years. The half-sib suicides on the right side of pedigree 5 are separated by 3 years.

References

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